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15,277 results for “GENETICS”
Figure 1 in Mitochondrial genetic variation within and between Holbrookia lacerata lacerata and Holbrookia lacerata subcaudalis, the spot-tailed earless lizards of Texas
Figure 1. Sampling map of the focal taxa (Holbrookia lacerata lacerata and H. l. subcaudalis) and outgroup taxa (H. maculata and H. propinqua). The sampling ranges for the nominal taxa are representative of their current distributions. The historical distribution of H. lacerata is represented by the dotted line, while the Balcones Fault/Escarpment, the natural biogeographic barrier between the two subspecies, is represented by the solid black line.
Figure 5 in Genetic and morphometric variation of the Blackcap (Sylvia atricapilla) on the Azores Archipelago reveals a recent range expansion
Figure 5. Morphological data: plot of the canonical discriminant analysis centroids (mean ± SD) of root 1 vs root 2 scores with the percentage of variance explained by each root. Axis units are scaled to the ratio of proportion of variance described by the roots. COR – Corvo; FLO – Flores; FAI – Faial; PIC – Pico; SJO – São Jorge; GRA – Graciosa; TER – Terceira; SMI – São Miguel; SMA – Santa Maria.
Figure 4 in Genetic and morphometric variation of the Blackcap (Sylvia atricapilla) on the Azores Archipelago reveals a recent range expansion
Figure 4. Bayesian skyline plot showing changes in effective population size through time (million years ago). Estimations were based on a molecular clock of 2% divergence for one million years. The population size and the generation time is reported on the y-axis. Estimates of means are joined by a solid line; whereas clear lines mark the 95% highest probability density limits.
Figure 2 in Genetic and morphometric variation of the Blackcap (Sylvia atricapilla) on the Azores Archipelago reveals a recent range expansion
Figure 2. Parsimony haplotype networks based on mtDNA (Cytb and Nd2 sequences) and Aco1 nuclear gene sequences of Blackcaps. Each circle represents a haplotype. Dots on lines represent the number of mutational steps between two haplotypes. C – Corvo; F – Flores; L – Faial; P – Pico; J – São Jorge; G – Graciosa; T – Terceira: S – São Miguel; M Santa Maria.
Figure 2 in Repeated sampling adds to the genetic diversity of Lepidochelys olivacea (Eschscholtz 1829) olive ridley sea turtle
Figure 2. Map of sea turtle migration for five tagged olive ridley sea turtles nesting on Campamento Tortuguero La Gloria, Jalisco, Mexico. Sea turtles with haplotype MLK are observed swimming into the pelagic zone in a south-southwest direction, and along the coast (solid line). The single sea turtle with the haplotype MLN also swam in a south-southwest direction (dotted line).
Figure 1. Haplotype network derived from 704 in Repeated sampling adds to the genetic diversity of Lepidochelys olivacea (Eschscholtz 1829) olive ridley sea turtle
Figure 1. Haplotype network derived from 704 bp mitochondrial D-loop fragment. Circle sizes are proportional to the frequency of each haplotype. The black circles are hypothetical haplotypes not sampled. Each colour represents the ocean basin where the sample was taken: blue is Pacific Ocean, yellow is Indian Ocean, red is Atlantic Ocean, and green is Indo-Pacific Ocean.
Figure 1 in Not as clear as expected: what genetic data tell about Southern Hemisphere corellids (Ascidiacea: Phlebobranchia)
Figure 1. Haplotype network for corellid species from COI data. Localities where the haplotypes have been found are indicated in shaded polygons. Areas of the circles are proportional to the number of haplotypes. Small white crossed dots without name represent missing, probably unsampled, haplotypes or extinct sequences. Dots along the lines between circles represent one mutational step. For haplotype ID see Figure 2. Ce: Corella eumyota; Ca: Corella antarctica; Cs: Corynascidia suhmi.
Figure 2 in Not as clear as expected: what genetic data tell about Southern Hemisphere corellids (Ascidiacea: Phlebobranchia)
Figure 2. Maximum parsimony strict consensus tree of partial COI gene analysis. A total of 15 equally parsimonious trees were obtained (975 length; consistency index: 0.689; retention index: 0.767). Branches retrieved by the three methods are indicated by three support values on the nodes. Values represent bootstrap supports when> 50% for MP and ML analyses and posterior probabilities for BI when> 0.5, in that order. Hyphen (-) denotes <50% bootstrap values and posterior probabilities <0.5; underscore (_) indicates the nodes that did not appear in the tree. Specimen haplotype IDs and GenBank sequences or BOLD System accession numbers are shown.
Figure 4 in Complete mitogenome of Chinese shrew mole Uropsilus soricipes (Milne- Edwards, 1871) (Mammalia: Talpidae) and genetic structure of the species in the Jiajin Mountains (China)
Figure 4. Expected (solid line) and observed (broken lines) mismatch distribution of Uropsilus soricipes based on cyt b. The x-axis represents the numbers of pairwise differences among sequences and the y-axis represents the relative frequencies of pairwise comparisons. (A) All individuals; (B) Jiajin Mountains population.
Figure 3. Bayesian 50 in Complete mitogenome of Chinese shrew mole Uropsilus soricipes (Milne- Edwards, 1871) (Mammalia: Talpidae) and genetic structure of the species in the Jiajin Mountains (China)
Figure 3. Bayesian 50% majority rule consensus phylogenetic tree of Eulipotyphla species from a phylogenetic analysis by the concatenated nucleotide sequences of 12 heavy strand proteincoding genes. Rattus rattus and Tupaia belangeri used as outgroup. The numbers on the internode branche is bootstrap percentages for ML analyses.
Figure 1 in Complete mitogenome of Chinese shrew mole Uropsilus soricipes (Milne- Edwards, 1871) (Mammalia: Talpidae) and genetic structure of the species in the Jiajin Mountains (China)
Figure 1. Study area and sampling sites for Chinese shrew mole (Uropsilus soricipes) in this study. Sample sizes can be found in Table 1.
Figure 5. Bayesian inference tree using the TIM2 in Complete mitogenome of Chinese shrew mole Uropsilus soricipes (Milne- Edwards, 1871) (Mammalia: Talpidae) and genetic structure of the species in the Jiajin Mountains (China)
Figure 5. Bayesian inference tree using the TIM2 + I + G model depicting the relationship of Uropsilus soricipes. The phylogenetic tree was rooted using Rattus rattus and Neotetracus sinensis. Numbers represent node supports inferred from Bayesian posterior probabilities. Clade A. Jiajin Mountains (JM); Dujiangyan (DJY); Tianquan (TQ); Maoxian (MX); Lixian (LX); Jiuzhaigou (JZG); Clade B. Yuexi (YX).
Figure 10. Pairwise 12S in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 10. Pairwise 12S rRNA sequence divergence within the americanus–robustus–vernalis complex. Genetic distance (Kimura 2-parameter) is compared between and within the four clades depicted in the tree of Figure 9. Note: Columns indicate mean values and bars indicate range (min.–max.).
Figure 6 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 6. Acanthocyclops americanus (Marsh) female neotype (A–C) and male allotype (4) from the terra typica, Madison, Wisconsin, USA. (A) Female Leg 5; (B) female antennal basipod frontal side; (C) female antennal basipod caudal side; (D) male Leg 4. Note: Scale bar 50 µm.
Figure 8 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 8. Pairwise COI sequence divergence within the americanus–robustus–vernalis complex. Genetic distance (Kimura 2-parameter) is compared between and within the three clades depicted in the tree of Figure 7. Note: Columns indicate mean values and bars indicate range (min.–max.).
Figure 7 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 7. Phylogenetic relationships based on maximum-likelihood analysis of mitochondrial COI sequences. Numbers beside nodes indicate bootstrap support values>70%. Individuals are identified by locality and the haplotype name is added if there more than one haplotype in the same locality. Notes: Haplotype names a1-a10 correpond to COIa1-COIa10 and vernalis 1–5 to COIv1-COIv5 from Table 1 and Figure 9; a map showing the geographical position of sampled areas and the number of localities in each area is shown in the top left part of the figure.
Figure 4 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 4. Acanthocyclops americanus (Marsh) female neotype from the terra typica, Madison, Wisconsin, USA. (A) Antennule; (B) antenna; (C) mandible; (D) maxillule; (E) maxilla; (F) maxilliped. Note: Scale bar = 50 µm.
Figure 5 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 5. Acanthocyclops americanus (Marsh) female neotype from the terra typica, Madison, Wisconsin, USA. (A–D) Swimming legs 1–4, in order. Note: Scale bar = 50 µm.
Figure 3 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 3. Acanthocyclops americanus (Marsh) from the terra typica, Madison, Wisconsin, USA. (A–B) Female neotype; (C) male allotype. Notes: Scale bar = 200 µm; neotype and allotype are from same samples used for molecular genetics, registered in Table 1, as are those in Figures 4–6).
Figure 2 in Molecular-genetic-based contribution to the taxonomy of the Acanthocyclops robustus group
Figure 2. Acanthocyclops robustus (Sars) female (A–F) and male (G–H) from the type locality, Lake Maridalsvann Oslo, Norway. (A) Leg 5 and genital segment in ventral view; (B) furca; (C) antennal basipod frontal side (D) antennal basipod caudal side; (E) Leg 4; (G) Leg4 distal segment of endopod; (H) Leg 4 endopod and exopod. Notes: All from the same samples used for molecular genetics, registered in Table 1.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.